| Weight | 285.235 g/mol |
|---|---|
| Formula | C10H12FN5O4 |
| Hydrogen Acceptors | 9 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
2-Fluoroadenosine (146-78-1)
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- 2-fluoroadenosine 3'.5'-monophosphate, A metabolite of 2-fluoroadenosine in mouse cytotoxic lymphocytes. (Journal of Biological Chemistry, 1976)
- A convenient method for the synthesis of 2-fluoroadenosine. (Journal of Organic Chemistry, 1968)
- Metabolism of 2-fluoroadenosine by Ehrlich ascites cells (Archives of Biochemistry and Biophysics, 1965)
- 2-deoxy4-C-ethynyl-2-fluoroadenosine, a nucleoside reverse transcriptase inhibitor, is highly potent against all human immunodeficiency viruses type 1 and has low toxicity (Chemical Record, 2006)
- 2-Deoxy-4-C-Ethynyl-2-Fluoroadenosine: A Nucleoside Reverse Transcriptase Inhibitor with Highly Potent Activity Against Wide Spectrum of HIV-1 Strains, Favorable Toxic Profiles, and Stability in Plasma (Nucleosides, Nucleotides & Nucleic Acids, 2007)
- Synergistic inhibition of platelet aggregation by forskolin plus PGE1 or 2-fluoroadenosine: Effects 2,5-dideoxyadenosine and 5-methylthioadenosine (Biochemical Pharmacology, 1982)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=NC2=C(N1C3C(C(C(O3)CO)O)O)N=C(N=C2N)F
-
InChIKeyHBUBKKRHXORPQB-UHFFFAOYSA-N
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